A novel protein polymorphism of human complement C7 detected by a monoclonal antibody

Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub-Saharan Africa: implications for the susceptibility to meningococcal disease.

Clinical and experimental immunology·2017

Complement component C5 and C6 mutation screening indicated in meningococcal disease in South Africa.

South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde·2012

Complete deficiency of the sixth complement component (C6Q0), susceptibility to Neisseria meningitidis infections and analysis of the frequencies of C6Q0 gene defects in South Africans.

Clinical and experimental immunology·2012

Characterization of a large genomic deletion in four Irish families with C7 deficiency.

Molecular immunology·2011

Complement-mediated lipopolysaccharide release and outer membrane damage in Escherichia coli J5: requirement for C9.

Immunology·2001

Reference typing report for complement components C6, C7 and C9 including mutations leading to deficiencies.

Experimental and clinical immunogenetics·1999

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Immunogenetics·2026

Genetic association of immunosenescence to immune decline.

Immunogenetics·2026

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Immunogenetics·2026

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Immunogenetics·2026

Elevated interleukin-36γ and gene polymorphisms implicate novel risk in essential hypertension.

Immunogenetics·2026

Unraveling the genomic structures, conserved functional domains and evolutionary dynamics of beta-defensins in Bubalus bubalis and Ovis aries.

Immunogenetics·2026

Sarsasapogenin Preserves Podocyte Integrity and Attenuates Renal Injury in Experimental IgA Nephropathy.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2026

Inherited Predisposition to Increased Systemic Inflammation Predicts a Broad Class of Disease Phenotypes.

HGG advances·2026

Growth differentiation factor 15 in common variable immunodeficiency patients: Diagnostic value and prediction of autoimmunity risk.

Allergy and asthma proceedings·2026

Protective effect of miR-642b-3p against brain injury after intracerebral hemorrhage by targeting SERPINE1.

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association·2026

Development of a High-Sensitivity Glycoproteomics Approach for Fc-Specific Quantification of IgG Core Fucosylation in Traumatic Brain Injury.

Journal of proteome research·2026

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Journal of clinical nursing·2026

Related Experiment Videos

A novel protein polymorphism of human complement C7 detected by a monoclonal antibody

Related Concept Videos

Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub-Saharan Africa: implications for the susceptibility to meningococcal disease.

Complement component C5 and C6 mutation screening indicated in meningococcal disease in South Africa.

Complete deficiency of the sixth complement component (C6Q0), susceptibility to Neisseria meningitidis infections and analysis of the frequencies of C6Q0 gene defects in South Africans.

Characterization of a large genomic deletion in four Irish families with C7 deficiency.

Complement-mediated lipopolysaccharide release and outer membrane damage in Escherichia coli J5: requirement for C9.

Reference typing report for complement components C6, C7 and C9 including mutations leading to deficiencies.

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Genetic association of immunosenescence to immune decline.

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Elevated interleukin-36γ and gene polymorphisms implicate novel risk in essential hypertension.

Unraveling the genomic structures, conserved functional domains and evolutionary dynamics of beta-defensins in Bubalus bubalis and Ovis aries.

Sarsasapogenin Preserves Podocyte Integrity and Attenuates Renal Injury in Experimental IgA Nephropathy.

Inherited Predisposition to Increased Systemic Inflammation Predicts a Broad Class of Disease Phenotypes.

Growth differentiation factor 15 in common variable immunodeficiency patients: Diagnostic value and prediction of autoimmunity risk.

Protective effect of miR-642b-3p against brain injury after intracerebral hemorrhage by targeting SERPINE1.

Development of a High-Sensitivity Glycoproteomics Approach for Fc-Specific Quantification of IgG Core Fucosylation in Traumatic Brain Injury.

Association Between Fluid Overload and Pressure Injuries in ICU Patients With Sepsis: A Retrospective Cohort Study.

Related Experiment Videos

A novel protein polymorphism of human complement C7 detected by a monoclonal antibody

Related Concept Videos

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